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Codman® Bactiseal®

FDA UDI

Class II (US FDA UDI)

by Integra LifeSciences Production Corporation

Identity

Trade Name
CODMAN® BACTISEAL® FDA UDI
Generic Name
Peritoneal/atrial cerebrospinal fluid catheter FDA UDI
Device Name
CODMAN® BACTISEAL® Distal Catheter Kit with BACTISEAL Shunt System MR CONDITIONAL Contents: Distal Catheter 120cm (1) FDA UDI
Model / Reference
823074 FDA UDI
Description
CODMAN® BACTISEAL® Distal Catheter Kit with BACTISEAL Shunt System MR CONDITIONAL Contents: Distal Catheter 120cm (1) FDA UDI

Identifiers

Catalog Number
82-3074 FDA UDI
Primary DI / UDI-DI
10381780537007 FDA UDI
FDA Product Code
JXG FDA UDI
HCA FDA UDI
GMDN Term
Peritoneal/atrial cerebrospinal fluid catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5550 FDA UDI
882.4100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Catheter Length — 120 Centimeter FDA UDI

Category: Peritoneal/atrial cerebrospinal fluid catheter

Codman® Bactiseal® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal/atrial cerebrospinal fluid catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eef04658-5f19-4674-8906-d72da4786c02 37 fields · synced Jun 9, 2026